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Body DissatisfactionBABINCT07422571

Body Acceptance After Baby Intervention

A study testing Body Acceptance after Baby (BABI) and Postpartum Body Image Infographic in people with Body Dissatisfaction, run by Northeastern University at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The purpose of this study is to learn if a novel online single-session intervention can help improve body dissatisfaction in new moms. The active intervention condition, Body Acceptance After Baby (BABI), uses acceptance-based skills to help participants cope with body dissatisfaction. Read more about this study

Who is it for?
Ages 18 years and older, women only
Conditions the study is for
Body Dissatisfaction
What is being tested?
Body Acceptance after Baby (BABI) and Postpartum Body Image Infographic
Could I receive a placebo?
No, everyone receives an active treatment
How many people
375 participants
Where
1 siteUnited States
Study dates
20 Jan 2026to Dec 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Individuals must:

  • Be currently residing in the U.S.
  • Be able to read and write in English
  • Be aged 18 or above
  • Identify as a woman
  • Have given birth to a live infant in the past year
  • Endorse dissatisfaction with their appearance (i.e., in answering the question "Indicate how satisfied you are with your overall appearance" they must answer neutral, mostly dissatisfied, or very dissatisfied)

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Rachel Rodgers, PhD contact

617 373 2105

r.rodgers@northeastern.edu

United States1 site, 1 recruiting
  • Northeastern University

    Boston, Massachusetts, 02115

    Rachel Rodgers, PhD, 617-470-9974, r.rodgers@northeastern.edu

    Recruiting

Other trials in United States

About this study

The purpose of this study is to learn if a novel online single-session intervention can help improve body dissatisfaction in new moms. The active intervention condition, Body Acceptance After Baby (BABI), uses acceptance-based skills to help participants cope with body dissatisfaction. BABI will be evaluated against another active intervention condition (a brief infographic that provides psychoeducation about body image during postpartum) and a waitlist control condition.

Being tested
Body Acceptance after Baby (BABI), Postpartum Body Image Infographic
Keywords
Body dissatisfaction, Postpartum, Single-session intervention, Acceptance and commitment therapy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Body Acceptance after Baby (BABI)Behavioural

    BABI is an online, self-directed single-session intervention designed to improve body dissatisfaction in postpartum moms (up to one year after delivery) aged 18 or older.

  • Postpartum Body Image InfographicBehavioural

    The postpartum body image infographic is an online pamphlet that provides psychoeducation about body image during postpartum.

Study groups in NCT07422571
Study groupRoleWhat they receive
Body Acceptance After Baby Intervention (BABI)ExperimentalThe active condition, BABI, includes (1) psychoeducation about body image during postpartum; (2) psychoeducation about acceptance; (3) an activity to practice "unhooking" (cognitive defusion skill); (4) a values clarification exercise; (5) a peer advice activity (participants give advice in response to vignettes of new moms who are struggling with body image); and (6) the creation of a personalized action plan. BABI is designed to take approximately 30 minutes.
Receives: Behavioral: Body Acceptance after Baby (BABI)
Postpartum Body Image InfographicExperimentalParticipants will read a brief infographic that includes (1) psychoeducation about body image and the harms of "bounce-back" culture during postpartum and (2) ways to improve body image. This infographic is designed to be read in approximately 2 minutes.
Receives: Behavioral: Postpartum Body Image Infographic
Waitlist ControlNo interventionThis group will receive no intervention, but will be given access to both active conditions at the end of follow-ups.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Postpartum body image

    Postpartum body image will be measured using the Body Image in Pregnancy Scale adapted for postpartum. Only the following subscales will be measured: (1) Preoccuptation with Physical Appearance; (2) Prioritization of Appearance over Function; (3) Appearance-Related Behavioral Avoidance. Subscales range from 1-5 with higher scores indicating greater body image disturbance.

    Measured: Baseline, 1 month, 3 months

Secondary outcomes (9)
  1. Body appreciation

    Body Appreciation will be measured using The Body Appreciation Scale-2 Short Form. Scores range from 3-15 with higher scores indicating greater body appreciation.

    Measured: Baseline, 1 month, 3 months

  2. Psychological flexibility

    Psychological flexibility will be measured with the Comprehensive assessment of Acceptance and Commitment Therapy processes (CompACT). Scores range from 0-138 with higher scores indicating greater psychological flexibility. Subscales can also be calculated to measure (1) Openness to Experience, (2) Behavioral Awareness, and (3) Valued Action.

    Measured: Baseline, 1 month, 3 months

  3. Postpartum depression

    Postpartum depression will be measured with the Edinburgh Postnatal Depression Scale (EPDS). Scores range from 0-30 with higher scores indicating greater depressive symptoms.

    Measured: Baseline, 1 month, 3 months

  4. Eating disorder symptoms

    Eating disorder symptoms will be measured with the Eating Disorder Examination Questionnaire Short (EDE-QS). Scores range from 0-36 with higher scores indicating greater severity of eating disorder symptoms.

    Measured: Baseline, 1 month, 3 months

  5. Intuitive eating

    Intuitive eating will be measured with the Intuitive Eating Scale-3 (IES-3) . Each item ranges from 1-5 and can be averaged to obtain a global score with higher scores indicating greater intuitive eating. Subscale scores (Unconditional Permission to Eat; Eating for Physical Reasons; Reliance on Hunger and Satiety Cues; Body-Food Choice Congruence) can also be calculated.

    Measured: Baseline, 1 month, 3 months

  6. Breastfeeding self-efficacy

    Breastfeeding self-efficacy will be measured with the Breastfeeding Self-Efficacy Scale (BSES-SF). Scores range from 14-70 with higher scores indicating greater self-efficacy.

    Measured: Baseline, 1 month, 3 months

  7. Bottle-feeding self-efficacy

    Bottle-feeding self-efficacy will be measured with the Bottle Feeding Self-Efficacy Scale. Scores range from 20-100 with higher scores indicating greater self-efficacy.

    Measured: Baseline, 1 month, 3 months

  8. State mood and body image

    Visual analog scales will be used to measure state anxiety, negative affect, positive affect, appearance satisfaction, weight satisfaction, muscle tone satisfaction, confidence, body acceptance, body positivity, anger, body functionality appreciation, body appreciation, broad concept of beauty (body sizes and body shapes) and body positive protective filter. Each item ranges from 0-100 with greater scores indicating greater levels of the respective variable.

    Measured: Baseline

  9. Hopelessness

    Hopelessness will be measured with the Beck Hopelessness Scale - 4-item version (BHS). Each item ranges from 0-3. Items are averaged to obtain a total score with higher scores indicating greater hopelessness.

    Measured: Baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Feb 2026
  2. Study start20 Jan 2026
  3. Primary completionDec 2027 (estimated)
  4. Study completionDec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
375 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07422571
Sponsor's protocol ID
24-11-25
Acronym
BABI
Status last verified
Feb 2026
First submitted
14 Nov 2025
Last updated
20 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Body Acceptance after Baby (BABI) and Postpartum Body Image Infographic in people with Body Dissatisfaction, run by Northeastern University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 20 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Rachel Rodgers, PhD (617 373 2105, r.rodgers@northeastern.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Postpartum body image (time frame: Baseline, 1 month, 3 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Feb 2026.

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